Behr Syndrome - Complicated hereditary infantile optic atrophy

Kleffner I., Meyer C., Gess B., Korsukewitz C., Allkemper T., Schirmacher A., Young P., Husstedt I. (2013)
In: Klinische Neurophysiologie, 44(1)
Type of Publication: Research article (journal)

Enhanced rapid-onset cortical plasticity in CADASIL as a possible mechanism of preserved cognition.

List J, Duning T, Meinzer M, Kürten J, Schirmacher A, Deppe M, Evers S, Young P, Flöel A (2011)
In: Cerebral cortex, 21(12)
Type of Publication: Research article (journal)

A novel splice site mutation in the SPG7 gene causing widespread fiber damage in homozygous and heterozygous subjects.

Warnecke T, Duning T, Schirmacher A, Mohammadi S, Schwindt W, Lohmann H, Dziewas R, Deppe M, Ringelstein EB, Young P (2010)
In: Movement Disorders, 25(4)
Type of Publication: Research article (journal)

Four novel mutations of the myelin protein zero gene presenting as a mild and late-onset polyneuropathy.

Kleffner I, Schirmacher A, Gess B, Boentert M, Young P (2010)
In: Journal of Neurology, 257(11)
Type of Publication: Research article (journal)

Mutations in SEPT9 cause hereditary neuralgic amyotrophy.

Kuhlenbäumer G, Hannibal MC, Nelis E, Schirmacher A, Verpoorten N, Meuleman J, Watts GD, De Vriendt E, Young P, Stögbauer F, Halfter H, Irobi J, Goossens D, Del-Favero J, Betz BG, Hor H, Kurlemann G, Bird TD, Airaksinen E, Mononen T, Serradell AP, Prats JM, Van Broeckhoven C, De Jonghe P, Timmerman V, Ringelstein EB, Chance PF (2005)
In: Nature Genetics, 37(10)
Type of Publication: Research article (journal)

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Behr Syndrome - Complicated hereditary infantile optic atrophy Kleffner I., Meyer C., Gess B., Korsukewitz C., Allkemper T., Schirmacher A., Young P., Husstedt I. (2013) In: Klinische Neurophysiologie, 44(1) Type of Publication: Research article (journal)
Interaction of BDNF and COMT polymorphisms on paired-associative stimulation-induced cortical plasticity. Witte AV, Kürten J, Jansen S, Schirmacher A, Brand E, Sommer J, Flöel A (2012) In: Journal of Neuroscience, 32(13) Type of Publication: Research article (journal)
Enhanced rapid-onset cortical plasticity in CADASIL as a possible mechanism of preserved cognition. List J, Duning T, Meinzer M, Kürten J, Schirmacher A, Deppe M, Evers S, Young P, Flöel A (2011) In: Cerebral cortex, 21(12) Type of Publication: Research article (journal)
Specific pattern of early white-matter changes in pure hereditary spastic paraplegia. Duning T, Warnecke T, Schirmacher A, Schiffbauer H, Lohmann H, Mohammadi S, Young P, Deppe M (2010) In: Movement Disorders, 25(12) Type of Publication: Research article (journal)
A novel splice site mutation in the SPG7 gene causing widespread fiber damage in homozygous and heterozygous subjects. Warnecke T, Duning T, Schirmacher A, Mohammadi S, Schwindt W, Lohmann H, Dziewas R, Deppe M, Ringelstein EB, Young P (2010) In: Movement Disorders, 25(4) Type of Publication: Research article (journal)
Autosomal-dominant striatal degeneration is caused by a mutation in the phosphodiesterase 8B gene. Appenzeller S, Schirmacher A, Halfter H, Bäumer S, Pendziwiat M, Timmerman V, De Jonghe P, Fekete K, Stögbauer F, Lüdemann P, Hund M, Quabius ES, Ringelstein EB, Kuhlenbäumer G (2010) In: American Journal of Human Genetics, 86(1) Type of Publication: Research article (journal)
Four novel mutations of the myelin protein zero gene presenting as a mild and late-onset polyneuropathy. Kleffner I, Schirmacher A, Gess B, Boentert M, Young P (2010) In: Journal of Neurology, 257(11) Type of Publication: Research article (journal)
Norepinephrine transporter (NET) promoter and 5'-UTR polymorphisms: association analysis in panic disorder. Lee YJ, Hohoff C, Domschke K, Sand P, Kuhlenbäumer G, Schirmacher A, Freitag CM, Meyer J, Stöber G, Franke P, Nöthen MM, Fritze J, Fimmers R, Garritsen HS, Stögbauer F, Deckert J (2005) In: Neuroscience Letters, 377(1) Type of Publication: Research article (journal)
Mutations in SEPT9 cause hereditary neuralgic amyotrophy. Kuhlenbäumer G, Hannibal MC, Nelis E, Schirmacher A, Verpoorten N, Meuleman J, Watts GD, De Vriendt E, Young P, Stögbauer F, Halfter H, Irobi J, Goossens D, Del-Favero J, Betz BG, Hor H, Kurlemann G, Bird TD, Airaksinen E, Mononen T, Serradell AP, Prats JM, Van Broeckhoven C, De Jonghe P, Timmerman V, Ringelstein EB, Chance PF (2005) In: Nature Genetics, 37(10) Type of Publication: Research article (journal)
Association of migraine with genetic variants of the NOTCH3 gene Evers S, Schwaag S, Frese A, Schirmacher A, Kuhlenbaumer G (2005) In: Cephalalgia, 25(10) Type of Publication: Research article (journal)